Canonical Allele Identifier: PA2826330524
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134304
ClinVar RCV Id: RCV000120977 RCV000205371 RCV000432064 RCV000575908 RCV000988218 RCV001095332 RCV001355214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gly139Glu
CA159408
NM_001243743.2:c.416G>A