Canonical Allele Identifier: PA2829391791
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 184411
ClinVar Variation Id: 926172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Gly3Arg
CA188884
NM_002876.4:c.7G>A
CA400336093
NM_002876.4:c.7G>C