Allele Registry

Canonical Allele Identifier: PA2826619484

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000004898

ClinVar Variation:

4635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267470.1:p.Val494Gly	CA340274 NM_001280541.2:c.1481T>G