Canonical Allele Identifier: PA2826156802
Gene: IFT80 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941741
ClinVar RCV Id: RCV002675703 RCV004066751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177171.1:p.Arg358Gln
CA355192065
NM_001190242.2:c.1073G>A