Canonical Allele Identifier: PA2829391856
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 631170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg12Gln
CA400336438
NM_002876.4:c.35G>A