Canonical Allele Identifier: PA916055717
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 825659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gln178Arg
CA400345207
NM_058216.3:c.533A>G