Canonical Allele Identifier: PA2828484337
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1337344
ClinVar RCV Id: RCV001820358 RCV002542613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361194.1:p.Arg181Gln
CA351618376
NM_001374265.1:c.542G>A