Allele Registry

Canonical Allele Identifier: PA2828493195

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000501246

RCV001150849

RCV001150850

RCV001150851

ClinVar Variation:

436395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361195.1:p.Glu51Lys	CA2258106 NM_001374266.1:c.151G>A