Allele Registry

Canonical Allele Identifier: PA645433663

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000501246

RCV001150849

RCV001150850

RCV001150851

ClinVar Variation:

436395

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Glu79Lys	CA2258106 NM_015869.4:c.235G>A