Canonical Allele Identifier: PA2829391909
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 187712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser20Cys
CA198382
NM_002876.4:c.59C>G