Allele Registry

Canonical Allele Identifier: PA645433569

Gene: BRIP1 HGNC NCBI

ClinVar Variation Id: 419651

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.His478Tyr	CA8690743 NM_032043.3:c.1432C>T