Allele Registry

Canonical Allele Identifier: PA099180

Gene: PPARG HGNC NCBI

ClinVar Variation Id: 8141

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Phe388Leu	CA119326 NM_015869.4:c.1164T>A CA351619865 NM_015869.4:c.1162T>C CA351619868 NM_015869.4:c.1164T>G