Canonical Allele Identifier: PA2829570470
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436402
ClinVar RCV Id: RCV000503417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005028.5:p.Glu349Lys
CA351619804
NM_005037.7:c.1045G>A