Allele Registry

Canonical Allele Identifier: PA2826620346

Gene: IFT122 HGNC NCBI

ClinVar RCV:

RCV000288140

ClinVar Variation:

343244

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267475.1:p.His377Gln	CA2606281 NM_001280546.2:c.1131C>G CA354477243 NM_001280546.2:c.1131C>A