Allele Registry

Canonical Allele Identifier: PA356894

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000206440

RCV000478530

RCV000567628

ClinVar Variation:

219651

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asn98Ser	CA350472 NM_032043.3:c.293A>G