Allele Registry

Canonical Allele Identifier: PA645433247

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000213526

RCV001051721

RCV002466471

ClinVar Variation:

230722

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ala349Ser	CA10580847 NM_032043.3:c.1045G>T