Allele Registry

Canonical Allele Identifier: PA2827915207

Gene: PPARG HGNC NCBI

ClinVar Allele:

135465

ClinVar RCV:

RCV000118044

RCV000300998

RCV000336176

RCV000406618

RCV001516919

ClinVar Variation:

130019

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341597.1:p.Pro12Ala	CA154763 NM_001354668.2:c.34C>G