Canonical Allele Identifier: PA2826619972
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_001267474.1:p.Gly422Val
CA236202
NM_001280545.2:c.1265G>T