Allele Registry

Canonical Allele Identifier: PA913198910

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000776784

ClinVar Variation:

630785

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Glu458Gln	CA400482259 NM_032043.3:c.1372G>C