Allele Registry

Canonical Allele Identifier: PA2827915378

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008620

ClinVar Variation:

8143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341599.1:p.Cys162Ser	CA119330 NM_001354670.2:c.484T>A CA351618443 NM_001354670.2:c.485G>C