Canonical Allele Identifier: PA2741839578
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2785117
ClinVar RCV Id: RCV003636171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ile276Thr
CA374109201
NM_001243744.2:c.827T>C