Canonical Allele Identifier: PA2829391947
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1014998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val25Ala
CA400336994
NM_002876.4:c.74T>C