Canonical Allele Identifier: PA2829570425
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1049745
ClinVar RCV Id: RCV001356245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005028.5:p.Gln269Arg
CA351619266
NM_005037.7:c.806A>G