Canonical Allele Identifier: PA2829391846
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1062191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Met10Thr
CA292046852
NM_002876.4:c.29T>C