Allele Registry

Canonical Allele Identifier: PA2829903989

Gene: IFT122 HGNC NCBI

ClinVar Variation Id: 195780

HGVS (amino-acid)	Matching Registered Transcripts
NP_060732.2:p.Tyr858Asp	CA209252 NM_018262.4:c.2572T>G