Allele Registry

Canonical Allele Identifier: PA916061907

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV001023668

ClinVar Variation:

825510

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg173Ser	CA400483405 NM_032043.3:c.517C>A