Canonical Allele Identifier: PA167876
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142245
ClinVar RCV Id: RCV000131254 RCV000461701 RCV003114285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg193Gln
CA167874
NM_058216.3:c.578G>A