Allele Registry

Canonical Allele Identifier: PA2827915227

Gene: PPARG HGNC NCBI

ClinVar Allele:

23169

ClinVar RCV:

RCV000008603

RCV002512915

ClinVar Variation:

8130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341597.1:p.Pro113Gln	CA119312 NM_001354668.2:c.338C>A