Allele Registry

Canonical Allele Identifier: PA2830261079

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008611

RCV004528094

ClinVar Variation:

8135

HGVS (amino-acid)	Matching Registered Transcripts
NP_619726.3:p.Arg286His	CA250559 NM_138712.5:c.857G>A