Allele Registry

Canonical Allele Identifier: PA2830132631

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000288140

ClinVar Variation:

343244

HGVS (amino-acid)	Matching Registered Transcripts
NP_443715.1:p.His586Gln	CA2606281 NM_052989.3:c.1758C>G CA354477243 NM_052989.3:c.1758C>A