Allele Registry

Canonical Allele Identifier: PA2829570438

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008613

ClinVar Variation:

8137

HGVS (amino-acid)	Matching Registered Transcripts
NP_005028.5:p.Val288Met	CA119321 NM_005037.7:c.862G>A