Canonical Allele Identifier: PA645460284
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 232017
ClinVar Variation Id: 2122635
ClinVar RCV Id: RCV003046966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Phe248Leu
CA10580750
NM_058216.3:c.742T>C
CA400353506
NM_058216.3:c.744T>G
CA400353515
NM_058216.3:c.744T>A