Canonical Allele Identifier: PA2828484136
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1706353
ClinVar RCV Id: RCV002284883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361193.2:p.Ser287Pro
CA351619387
NM_001374264.2:c.859T>C