Canonical Allele Identifier: PA2829392253
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 538766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.His82Arg
CA400340343
NM_002876.4:c.245A>G