Canonical Allele Identifier: PA645460263
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 232379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Glu232Asp
CA10580747
NM_058216.3:c.696A>T
CA400350114
NM_058216.3:c.696A>C