Allele Registry

Canonical Allele Identifier: PA645465456

Gene: IFT140 HGNC NCBI

ClinVar Variation Id: 318220

HGVS (amino-acid)	Matching Registered Transcripts
NP_055529.2:p.Gln8Glu	CA7814853 NM_014714.4:c.22C>G