Canonical Allele Identifier: PA2827915089
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1969349
ClinVar RCV Id: RCV002730087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341596.2:p.Ala61Thr
CA2258111
NM_001354667.3:c.181G>A