Allele Registry

Canonical Allele Identifier: PA645460452

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000288140

ClinVar Variation:

343244

HGVS (amino-acid)	Matching Registered Transcripts
NP_443711.2:p.His637Gln	CA2606281 NM_052985.4:c.1911C>G CA354477243 NM_052985.4:c.1911C>A