Canonical Allele Identifier: PA2828483879
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1337735
ClinVar RCV Id: RCV001822333
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Leu307Pro
CA351619526
NM_001374263.2:c.920T>C