Canonical Allele Identifier: PA2828493238
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_001361195.1:p.Ser158Gly
CA351618409
NM_001374266.1:c.472A>G