Canonical Allele Identifier: PA2826331656
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182485
ClinVar RCV Id: RCV000160486 RCV000477242 RCV000570128 RCV001273988 RCV001358089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Glu417Lys
CA299184
NM_001243743.2:c.1249G>A