Canonical Allele Identifier: PA2827915381
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1337832
ClinVar RCV Id: RCV001822430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341599.1:p.Ser176Pro
CA351618539
NM_001354670.2:c.526T>C