Allele Registry

Canonical Allele Identifier: PA916051674

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000004901

ClinVar Variation:

4638

HGVS (amino-acid)	Matching Registered Transcripts
NP_443716.1:p.Trp7Cys	CA340279 NM_052990.3:c.21G>C CA354469060 NM_052990.3:c.21G>T