Allele Registry

Canonical Allele Identifier: PA2830132497

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000272301

ClinVar Variation:

343235

HGVS (amino-acid)	Matching Registered Transcripts
NP_443715.1:p.Arg277Trp	CA2606009 NM_052989.3:c.829C>T