Canonical Allele Identifier: PA299903
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182842
ClinVar RCV Id: RCV000233682 RCV000587134 RCV000709500 RCV001189359
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gln11Arg
CA299901
NM_058216.3:c.32A>G