Canonical Allele Identifier: PA2828484061
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2175038
ClinVar RCV Id: RCV002578919
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361193.2:p.Ser156Gly
CA351618409
NM_001374264.2:c.466A>G