Canonical Allele Identifier: PA2827915377
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_001341599.1:p.Ser158Gly
CA351618409
NM_001354670.2:c.472A>G