Canonical Allele Identifier: PA2828483816
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436397
ClinVar RCV Id: RCV000499572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Arg164Gln
CA70181654
NM_001374263.2:c.491G>A