Allele Registry

Canonical Allele Identifier: PA2828483817

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008621

ClinVar Variation:

8144

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361192.2:p.Arg164Trp	CA119332 NM_001374263.2:c.490C>T