Canonical Allele Identifier: PA2741997087
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2695443
ClinVar RCV Id: RCV003507582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.His207Leu
CA400349388
NM_058216.3:c.620A>T