Allele Registry

Canonical Allele Identifier: PA2827915379

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008621

ClinVar Variation:

8144

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341599.1:p.Arg166Trp	CA119332 NM_001354670.2:c.496C>T