databases > bsg-d001810

ready AIP Mutation Database

General Information
The AIP Mutation Database collects variants (both pathogenic, non-pathogenic and with unknown significance) related to pituitary adenoma predisposition (PAP) and to familial isolated pituitary adenoma (FIPA) syndromes and their clinical information in order to understand better the molecular and clinical details of the disease. Variants are reported according to the GRCh37/hg19 assembly of the human genome and the reference sequence used is the AIP Locus Reference Genomic.

Homepage https://aip.fipapatients.org

Countries that developed this resource United Kingdom

Created in 2012

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Record added: March 5, 2021, 2:22 p.m.
Record updated: March 5, 2021, 2:33 p.m. by The FAIRsharing Team.

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support email Dr Giampaolo Trivellin
support email Dr Mary Dang
support email Prof Márta Korbonits
online documentation AIP Background

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Contact Dr Serban Radian

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