Canonical Allele Identifier: PA2573071426
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1337735
ClinVar RCV Id: RCV001822333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341598.1:p.Leu98Pro
CA351619526
NM_001354669.2:c.293T>C