Allele Registry

Canonical Allele Identifier: PA2827915303

Gene: PPARG HGNC NCBI

ClinVar Variation Id: 8141

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341598.1:p.Phe149Leu	CA119326 NM_001354669.2:c.447T>A CA351619865 NM_001354669.2:c.445T>C CA351619868 NM_001354669.2:c.447T>G