Canonical Allele Identifier: PA2827915166
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_001341596.2:p.Leu331Phe
CA2258308
NM_001354667.3:c.993G>C
CA351619686
NM_001354667.3:c.993G>T