Allele Registry

Canonical Allele Identifier: PA288572

Gene: BRIP1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000116149

RCV000199089

RCV000409338

RCV000411198

RCV000585934

RCV000855583

RCV001030467

RCV003315655

RCV003492507

RCV004529951

ClinVar Variation:

128180

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Gln944Glu	CA288570 NM_032043.3:c.2830C>G