Canonical Allele Identifier: PA2829391924
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1098885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ala22Val
CA400336839
NM_002876.4:c.65C>T