Allele Registry

Canonical Allele Identifier: PA2826619885

Gene: IFT122 HGNC NCBI

ClinVar Allele:

19675

ClinVar RCV:

RCV000004899

ClinVar Variation:

4636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267474.1:p.Ser172Phe	CA340276 NM_001280545.2:c.515C>T