Canonical Allele Identifier: PA645433667
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436397
ClinVar RCV Id: RCV000499572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056953.2:p.Arg194Gln
CA70181654
NM_015869.4:c.581G>A