Allele Registry

Canonical Allele Identifier: PA2828493183

Gene: PPARG HGNC NCBI

ClinVar Allele:

23170

ClinVar RCV:

RCV000008604

RCV000008605

RCV000008606

RCV000008607

ClinVar Variation:

8131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361195.1:p.Pro12Ala	CA119314 NM_001374266.1:c.34C>G