Canonical Allele Identifier: PA2573205330
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1607706
ClinVar RCV Id: RCV002144781
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Thr2Ile
CA432300170
NM_001354669.2:c.5C>T