Allele Registry

Canonical Allele Identifier: PA658663392

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000563546

RCV001372997

ClinVar Variation:

483156

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asn471Ser	CA400482165 NM_032043.3:c.1412A>G