Canonical Allele Identifier: PA2826334461
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 557891
ClinVar RCV Id: RCV000674090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ile492_Ter493insGlySerValIleAlaGlnLeuProTyrLeuProGlnGlyArgValLeuGlnGlyValProCysArgGlyGlyLeuPhe
CA374106593
NM_001243744.2:c.1477T>G