Allele Registry

Canonical Allele Identifier: PA298874

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000160336

RCV000565573

RCV001300398

ClinVar Variation:

182346

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ile359Met	CA298872 NM_032043.3:c.1077A>G