Canonical Allele Identifier: PA658670849
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 480947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg7His
CA292046832
NM_058216.3:c.20G>A