Canonical Allele Identifier: PA2826329953
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2450943
ClinVar RCV Id: RCV003171546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg439Gly
CA374107248
NM_001243743.2:c.1315A>G