Allele Registry

Canonical Allele Identifier: PA658663797

Gene: BRIP1 HGNC NCBI

ClinVar Variation Id: 479410

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asp1112Tyr	CA292267318 NM_032043.3:c.3334G>T