Canonical Allele Identifier: PA2828483892
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2780020
ClinVar RCV Id: RCV003665473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Leu328Pro
CA351619668
NM_001374263.2:c.983T>C