Canonical Allele Identifier: PA645460062
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Val15Gly
CA16615800
NM_058216.3:c.44T>G