Allele Registry

Canonical Allele Identifier: PA916010691

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000272301

ClinVar Variation:

343235

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267475.1:p.Arg68Trp	CA2606009 NM_001280546.2:c.202C>T