Allele Registry

Canonical Allele Identifier: PA645432156

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000217783

RCV000636140

RCV003441804

ClinVar Variation:

234145

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Tyr19Cys	CA10580898 NM_032043.3:c.56A>G