Allele Registry

Canonical Allele Identifier: PA2830079032

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV004519823

ClinVar Variation:

3228113

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser919Ala	CA400481600 NM_032043.3:c.2755T>G