Canonical Allele Identifier: PA2573067763
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1324376
ClinVar RCV Id: RCV001781081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Met1Thr