Allele Registry

Canonical Allele Identifier: PA658816865

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000636129

RCV000775419

ClinVar Variation:

530325

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg579His	CA8690680 NM_032043.3:c.1736G>A