Allele Registry

Canonical Allele Identifier: PA336893

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000564994

RCV000802648

RCV001307947

RCV001755930

ClinVar Variation:

216791

481628

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Cys87Ser	CA336891 NM_032043.3:c.260G>C CA400485515 NM_032043.3:c.259T>A