Canonical Allele Identifier: PA2828483904
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2867439
ClinVar RCV Id: RCV003702737
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Ser353Asp
CA2739277866
NM_001374263.2:c.1057_1058delinsGA