Canonical Allele Identifier: PA2580176538
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1793659
ClinVar RCV Id: RCV002437134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ser9Thr
CA374340504
NM_001243744.2:c.25T>A