Allele Registry

Canonical Allele Identifier: PA2828484132

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008609

ClinVar Variation:

8133

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361193.2:p.Gln284Pro	CA250555 NM_001374264.2:c.851A>C