Canonical Allele Identifier: PA2826330865
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456165
ClinVar RCV Id: RCV000552262 RCV001025378 RCV002483353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Glu218Gln
CA5137677
NM_001243743.2:c.652G>C