Canonical Allele Identifier: PA916039050
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436397
ClinVar RCV Id: RCV000499572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Gly22Ser
CA70181654
NM_001354669.2:c.64G>A