Allele Registry

Canonical Allele Identifier: PA645436220

Gene: BRIP1 HGNC NCBI

ClinVar Variation Id: 407813

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Glu1110Gly	CA16615483 NM_032043.3:c.3329A>G