Canonical Allele Identifier: PA2828493241
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436397
ClinVar RCV Id: RCV000499572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361195.1:p.Arg166Gln
CA70181654
NM_001374266.1:c.497G>A