Allele Registry

Canonical Allele Identifier: PA658809418

Gene: IFT140 HGNC NCBI

ClinVar Variation Id: 499715

HGVS (amino-acid)	Matching Registered Transcripts
NP_055529.2:p.Arg1403Gln	CA7812829 NM_014714.4:c.4208G>A