Allele Registry

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Canonical Allele Identifier: PA2573186611

Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1399718

ClinVar RCV Id: RCV001893869 RCV002397871

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Glu517Asp	CA374104796 NM_001243743.2:c.1551G>T CA374104797 NM_001243743.2:c.1551G>C