Allele Registry

Canonical Allele Identifier: PA645460440

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000272301

ClinVar Variation:

343235

HGVS (amino-acid)	Matching Registered Transcripts
NP_443711.2:p.Arg328Trp	CA2606009 NM_052985.4:c.982C>T