Canonical Allele Identifier: PA2830261077
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8133
ClinVar RCV Id: RCV000008609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619726.3:p.Gln284Pro
CA250555
NM_138712.5:c.851A>C