Canonical Allele Identifier: PA2580432573
Gene: IFT80 HGNC NCBI

Linked Data

ClinVar Variation Id: 2038756
ClinVar RCV Id: RCV002895191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065851.1:p.Phe496Leu
CA355192044
NM_020800.3:c.1488T>G
CA355192046
NM_020800.3:c.1488T>A
CA355192060
NM_020800.3:c.1486T>C