Allele Registry

Canonical Allele Identifier: PA645436141

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000215643

RCV000484982

RCV001087512

RCV001818520

ClinVar Variation:

230429

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Glu1027Lys	CA8690401 NM_032043.3:c.3079G>A