Canonical Allele Identifier: PA2829392517
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 478610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val129Ile
CA400341933
NM_002876.4:c.385G>A