Canonical Allele Identifier: PA891856351
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 581940
ClinVar RCV Id: RCV000705897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Asp318Tyr
CA400361541
NM_058216.3:c.952G>T