Canonical Allele Identifier: PA2830261005
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_619726.3:p.Ser174Pro
CA351618539
NM_138712.5:c.520T>C