Canonical Allele Identifier: PA2499295649
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1009003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ala35Ser
CA400337369
NM_058216.3:c.103G>T