Canonical Allele Identifier: PA915966721
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 771596
ClinVar RCV Id: RCV000950942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Arg1433His
CA7812794
NM_014714.4:c.4298G>A