Canonical Allele Identifier: PA2827337613
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436396
ClinVar RCV Id: RCV000503040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317544.2:p.Gly131Val
CA351618245
NM_001330615.4:c.392G>T