Allele Registry

Canonical Allele Identifier: PA2828483501

Gene: PPARG HGNC NCBI

ClinVar Allele:

23169

ClinVar RCV:

RCV000008603

RCV002512915

ClinVar Variation:

8130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361190.2:p.Pro83Gln	CA119312 NM_001374261.3:c.248C>A