Canonical Allele Identifier: PA913202216
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 627998
ClinVar RCV Id: RCV000772272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gln222His
CA400349838
NM_058216.3:c.666A>T
CA400349839
NM_058216.3:c.666A>C