Canonical Allele Identifier: PA2826331508
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 419389
ClinVar RCV Id: RCV000483173 RCV000806505 RCV002374890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Cys387Arg
CA16618880
NM_001243743.2:c.1159T>C