Allele Registry

Canonical Allele Identifier: PA916039052

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008611

RCV004528094

ClinVar Variation:

8135

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341598.1:p.Arg77His	CA250559 NM_001354669.2:c.230G>A