Canonical Allele Identifier: PA658671322
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 478781
ClinVar Variation Id: 822945
ClinVar RCV Id: RCV001018724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gly302Arg
CA400359832
NM_058216.3:c.904G>A
CA400359834
NM_058216.3:c.904G>C