Allele Registry

Canonical Allele Identifier: PA099168

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008619

RCV001818145

ClinVar Variation:

8142

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Arg425Cys	CA119328 NM_015869.4:c.1273C>T