Canonical Allele Identifier: PA2826330722
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 825878
ClinVar RCV Id: RCV001024376 RCV001276455 RCV001862286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Pro189Thr
CA5137691
NM_001243743.2:c.565C>A