Canonical Allele Identifier: PA2830260698
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_619725.3:p.Ser156Gly
CA351618409
NM_138711.6:c.466A>G