Allele Registry

Canonical Allele Identifier: PA916039053

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008613

ClinVar Variation:

8137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341598.1:p.Val79Met	CA119321 NM_001354669.2:c.235G>A