Allele Registry

Canonical Allele Identifier: PA2827915052

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008619

RCV001818145

ClinVar Variation:

8142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341595.2:p.Arg395Cys	CA119328 NM_001354666.3:c.1183C>T