Allele Registry

Canonical Allele Identifier: PA2829903467

Gene: IFT122 HGNC NCBI

ClinVar Variation Id: 530928

HGVS (amino-acid)	Matching Registered Transcripts
NP_060732.2:p.Asp359Asn	CA2606114 NM_018262.4:c.1075G>A