Canonical Allele Identifier: PA658670839
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 484753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr5Arg
CA8677119
NM_058216.3:c.14C>G