Canonical Allele Identifier: PA2580227628
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1706353
ClinVar RCV Id: RCV002284883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Ser78Pro
CA351619387
NM_001354669.2:c.232T>C