Canonical Allele Identifier: PA645460255
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 232604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu219Ser
CA8677291
NM_058216.3:c.656T>C