Canonical Allele Identifier: PA2830260702
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436397
ClinVar RCV Id: RCV000499572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619725.3:p.Arg164Gln
CA70181654
NM_138711.6:c.491G>A