Allele Registry

Canonical Allele Identifier: PA2827915045

Gene: PPARG HGNC NCBI

ClinVar Variation Id: 8141

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341595.2:p.Phe358Leu	CA119326 NM_001354666.3:c.1074T>A CA351619865 NM_001354666.3:c.1072T>C CA351619868 NM_001354666.3:c.1074T>G