Canonical Allele Identifier: PA2580176881
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1751526
ClinVar RCV Id: RCV002360074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Glu405Asp
CA5137420
NM_001243744.2:c.1215G>T
CA374107453
NM_001243744.2:c.1215G>C