Canonical Allele Identifier: PA2826329942
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127531
ClinVar RCV Id: RCV000115341 RCV000206060 RCV002381419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg433Cys
CA287184
NM_001243743.2:c.1297C>T