Canonical Allele Identifier: PA2826156795
Gene: IFT80 HGNC NCBI

Linked Data

ClinVar Variation Id: 2485850
ClinVar RCV Id: RCV003205535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177171.1:p.Arg340Gly
CA2685147
NM_001190242.2:c.1018A>G