Canonical Allele Identifier: PA2827915028
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1337735
ClinVar RCV Id: RCV001822333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341595.2:p.Leu307Pro
CA351619526
NM_001354666.3:c.920T>C