Canonical Allele Identifier: PA2825055386
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1738609
ClinVar RCV Id: RCV002327820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Tyr140Cys
CA374338771
NM_000136.3:c.419A>G