Allele Registry

Canonical Allele Identifier: PA658663668

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000565343

RCV001300400

ClinVar Variation:

483140

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser876Asn	CA8690468 NM_032043.3:c.2627G>A