Canonical Allele Identifier: PA645397424
Gene: IFT80 HGNC NCBI

Linked Data

ClinVar Variation Id: 406217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065851.1:p.Thr365Ala
CA2685255
NM_020800.3:c.1093A>G