Canonical Allele Identifier: PA2830260850
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_619725.3:p.Leu307Pro
CA351619526
NM_138711.6:c.920T>C