Allele Registry

Canonical Allele Identifier: PA645432152

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000216902

RCV000467101

RCV001354597

RCV003148687

ClinVar Variation:

232285

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Met4Val	CA10580900 NM_032043.3:c.10A>G