Allele Registry

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Canonical Allele Identifier: PA2826331592

Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 550052

ClinVar RCV Id: RCV000664675

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Trp403Arg	CA374107473 NM_001243743.2:c.1207T>C CA374107474 NM_001243743.2:c.1207T>A