Canonical Allele Identifier: PA658671205
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 484729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg214His
CA8677286
NM_058216.3:c.641G>A