Canonical Allele Identifier: PA2830133236
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 191184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443716.1:p.Gly461Val
CA236202
NM_052990.3:c.1382G>T