Canonical Allele Identifier: PA2830261104
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 3057846
ClinVar RCV Id: RCV004540973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619726.3:p.Leu331Phe
CA2258308
NM_138712.5:c.993G>C
CA351619686
NM_138712.5:c.993G>T