Canonical Allele Identifier: PA2580176477
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1773364
ClinVar RCV Id: RCV002396938 RCV003523133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu491Val
CA5137327
NM_001243743.2:c.1471C>G