Canonical Allele Identifier: PA658732793
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 492366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.His82Tyr
CA400340328
NM_058216.3:c.244C>T