Canonical Allele Identifier: PA2826330566
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1741614
ClinVar RCV Id: RCV002342181 RCV003476957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Met153Val
CA374338678
NM_001243743.2:c.457A>G