Canonical Allele Identifier: PA2828483873
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_001361192.2:p.Ile294Thr
CA351619437
NM_001374263.2:c.881T>C