Allele Registry

Canonical Allele Identifier: PA2830261084

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008613

ClinVar Variation:

8137

HGVS (amino-acid)	Matching Registered Transcripts
NP_619726.3:p.Val288Met	CA119321 NM_138712.5:c.862G>A