Allele Registry

Canonical Allele Identifier: PA2828483728

Gene: PPARG HGNC NCBI

ClinVar Allele:

23170

ClinVar RCV:

RCV000008604

RCV000008605

RCV000008606

RCV000008607

ClinVar Variation:

8131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361192.2:p.Pro10Ala	CA119314 NM_001374263.2:c.28C>G