Allele Registry

Canonical Allele Identifier: PA2828493258

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008619

RCV001818145

ClinVar Variation:

8142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361195.1:p.Pro219Leu	CA119328 NM_001374266.1:c.656C>T