Canonical Allele Identifier: PA916039052
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8135
ClinVar RCV Id: RCV000008611 RCV004528094
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Arg77His
CA250559
NM_001354669.2:c.230G>A