Allele Registry

Canonical Allele Identifier: PA288599

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000116158

RCV000200049

RCV000662347

RCV000662581

RCV001535683

RCV003150947

RCV003315659

ClinVar Variation:

128189

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Gly1155Glu	CA288597 NM_032043.3:c.3464G>A