Allele Registry

Canonical Allele Identifier: PA645436205

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000217837

RCV003765440

ClinVar Variation:

233788

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Leu1093Phe	CA10580779 NM_032043.3:c.3277C>T