Allele Registry

Canonical Allele Identifier: PA658663805

Gene: BRIP1 HGNC NCBI

ClinVar Variation Id: 483208

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser1115Cys	CA400478933 NM_032043.3:c.3344C>G