Canonical Allele Identifier: PA1139760256
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 962548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gln97Arg
CA400340907
NM_058216.3:c.290A>G