Allele Registry

Canonical Allele Identifier: PA2830133123

Gene: IFT122 HGNC NCBI

ClinVar Variation Id: 530928

HGVS (amino-acid)	Matching Registered Transcripts
NP_443716.1:p.Asp307Asn	CA2606114 NM_052990.3:c.919G>A