Canonical Allele Identifier: PA2830260863
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2780020
ClinVar RCV Id: RCV003665473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619725.3:p.Leu328Pro
CA351619668
NM_138711.6:c.983T>C