Allele Registry

Canonical Allele Identifier: PA2827915310

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008619

RCV001818145

ClinVar Variation:

8142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341598.1:p.Arg186Cys	CA119328 NM_001354669.2:c.556C>T