Canonical Allele Identifier: PA916039051
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8133
ClinVar RCV Id: RCV000008609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Gln75Pro
CA250555
NM_001354669.2:c.224A>C