Allele Registry

Canonical Allele Identifier: PA2829903467

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000637014

RCV001756057

RCV004025487

ClinVar Variation:

530928

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