Canonical Allele Identifier: PA2826330977
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758873
ClinVar RCV Id: RCV002385014 RCV003635988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Pro248Ser
CA5137642
NM_001243743.2:c.742C>T