Allele Registry

Canonical Allele Identifier: PA2573072780

Gene: PPARG HGNC NCBI

ClinVar Allele:

23169

ClinVar RCV:

RCV000008603

RCV002512915

ClinVar Variation:

8130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361195.1:p.Pro85Gln	CA119312 NM_001374266.1:c.254C>A