Allele Registry

Canonical Allele Identifier: PA2830260807

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008609

ClinVar Variation:

8133

HGVS (amino-acid)	Matching Registered Transcripts
NP_619725.3:p.Gln284Pro	CA250555 NM_138711.6:c.851A>C