Canonical Allele Identifier: PA2825055132
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1750957
ClinVar RCV Id: RCV002357944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ser20Cys
CA374340422
NM_000136.3:c.59C>G