Canonical Allele Identifier: PA2829570434
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_005028.5:p.Arg286His
CA250559
NM_005037.7:c.857G>A