Canonical Allele Identifier: PA2827915032
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2974355
ClinVar RCV Id: RCV003835993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341595.2:p.Val320Ile
CA70184221
NM_001354666.3:c.958G>A