Allele Registry

Canonical Allele Identifier: PA2828493240

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008620

ClinVar Variation:

8143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361195.1:p.Cys162Ser	CA119330 NM_001374266.1:c.484T>A CA351618443 NM_001374266.1:c.485G>C