Canonical Allele Identifier: PA658670967
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 486272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ile64Val
CA400339873
NM_058216.3:c.190A>G