Canonical Allele Identifier: PA2828483810
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2984411
ClinVar RCV Id: RCV003843570
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.His153Tyr
CA351618388
NM_001374263.2:c.457C>T