Canonical Allele Identifier: PA2829391847
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1797407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Met10Val
CA400336377
NM_002876.4:c.28A>G