Allele Registry

Canonical Allele Identifier: PA2826619422

Gene: IFT122 HGNC NCBI

ClinVar Allele:

19675

ClinVar RCV:

RCV000004899

ClinVar Variation:

4636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267470.1:p.Ser314Phe	CA340276 NM_001280541.2:c.941C>T