Canonical Allele Identifier: PA2829570414
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1508623
ClinVar RCV Id: RCV002016240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005028.5:p.Asn251Ser
CA70184215
NM_005037.7:c.752A>G