Canonical Allele Identifier: PA2827915021
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1706353
ClinVar RCV Id: RCV002284883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341595.2:p.Ser287Pro
CA351619387
NM_001354666.3:c.859T>C