Allele Registry

Canonical Allele Identifier: PA2828483616

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000501246

RCV001150849

RCV001150850

RCV001150851

ClinVar Variation:

436395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361191.2:p.Glu49Lys	CA2258106 NM_001374262.3:c.145G>A