Canonical Allele Identifier: PA645460072
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 229691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg24Gln
CA8677136
NM_058216.3:c.71G>A