Allele Registry

Canonical Allele Identifier: PA1139739581

Gene: IFT140 HGNC NCBI

ClinVar Variation Id: 886296

HGVS (amino-acid)	Matching Registered Transcripts
NP_055529.2:p.Ala437Thr	CA7814373 NM_014714.4:c.1309G>A