Allele Registry

Canonical Allele Identifier: PA2828484062

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008620

ClinVar Variation:

8143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361193.2:p.Cys160Ser	CA119330 NM_001374264.2:c.478T>A CA351618443 NM_001374264.2:c.479G>C