Canonical Allele Identifier: PA198384
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 187712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ser20Cys
CA198382
NM_058216.3:c.59C>G