Canonical Allele Identifier: PA333011
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 136161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu201Pro
CA333009
NM_058216.3:c.602T>C