Canonical Allele Identifier: PA2826333109
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230385
ClinVar RCV Id: RCV004520536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Leu155Ile
CA374338665
NM_001243744.2:c.463T>A