Canonical Allele Identifier: PA2580176478
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1773436
ClinVar RCV Id: RCV002397010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu492Val
CA374105724
NM_001243743.2:c.1474C>G