Canonical Allele Identifier: PA916039054
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436399
ClinVar RCV Id: RCV000503151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Ile85Thr
CA351619437
NM_001354669.2:c.254T>C