Allele Registry

Canonical Allele Identifier: PA2826619976

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000288140

ClinVar Variation:

343244

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267474.1:p.His436Gln	CA2606281 NM_001280545.2:c.1308C>G CA354477243 NM_001280545.2:c.1308C>A