Canonical Allele Identifier: PA2830153521
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1729179
ClinVar RCV Id: RCV002324728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Asp108Tyr
CA400341215
NM_058216.3:c.322G>T