Allele Registry

Canonical Allele Identifier: PA2827915020

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008611

RCV004528094

ClinVar Variation:

8135

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341595.2:p.Arg286His	CA250559 NM_001354666.3:c.857G>A