Allele Registry

Canonical Allele Identifier: PA2830133041

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000272301

ClinVar Variation:

343235

HGVS (amino-acid)	Matching Registered Transcripts
NP_443716.1:p.Arg166Trp	CA2606009 NM_052990.3:c.496C>T