Canonical Allele Identifier: PA2826156790
Gene: IFT80 HGNC NCBI

Linked Data

ClinVar Variation Id: 1498171
ClinVar RCV Id: RCV001996447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177171.1:p.Asp332Tyr
CA355192448
NM_001190242.2:c.994G>T