Allele Registry

Canonical Allele Identifier: PA167469

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

151841

ClinVar RCV:

RCV000130967

RCV000479209

RCV000636069

RCV003462006

RCV003479016

RCV004528857

ClinVar Variation:

142127

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ile550Met	CA167467 NM_032043.3:c.1650T>G