Canonical Allele Identifier: PA2826331728
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1768973
ClinVar RCV Id: RCV002383190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Tyr429Phe
CA374107306
NM_001243743.2:c.1286A>T