Canonical Allele Identifier: PA2827915119
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2175038
ClinVar RCV Id: RCV002578919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341596.2:p.Ser156Gly
CA351618409
NM_001354667.3:c.466A>G