Canonical Allele Identifier: PA2828484134
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_001361193.2:p.Arg286His
CA250559
NM_001374264.2:c.857G>A