Canonical Allele Identifier: PA236203
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 191184
ClinVar RCV Id: RCV000171370 RCV003989481
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443711.2:p.Gly623Val
CA236202
NM_052985.4:c.1868G>T