Allele Registry

Canonical Allele Identifier: PA2826620285

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000637014

RCV001756057

RCV004025487

ClinVar Variation:

530928

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267475.1:p.Asp209Asn	CA2606114 NM_001280546.2:c.625G>A