Canonical Allele Identifier: PA2828484002
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 3217014
ClinVar RCV Id: RCV004514877
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361193.2:p.Thr45Ala
CA70180289
NM_001374264.2:c.133A>G