Canonical Allele Identifier: PA658820223
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 538768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu38Pro
CA400337513
NM_058216.3:c.113T>C