Canonical Allele Identifier: PA658820241
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 538766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.His82Arg
CA400340343
NM_058216.3:c.245A>G