Allele Registry

Canonical Allele Identifier: PA2827915023

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008613

ClinVar Variation:

8137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341595.2:p.Val288Met	CA119321 NM_001354666.3:c.862G>A