Allele Registry

Canonical Allele Identifier: PA658663500

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000576027

RCV001858189

ClinVar Variation:

481637

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Thr632Ala	CA400479308 NM_032043.3:c.1894A>G