Canonical Allele Identifier: PA2828493242
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8144
ClinVar RCV Id: RCV000008621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361195.1:p.Arg166Trp
CA119332
NM_001374266.1:c.496C>T