Allele Registry

Canonical Allele Identifier: PA658819979

Gene: IFT122 HGNC NCBI

ClinVar Variation Id: 530928

HGVS (amino-acid)	Matching Registered Transcripts
NP_443711.2:p.Asp469Asn	CA2606114 NM_052985.4:c.1405G>A