Canonical Allele Identifier: PA2828483864
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8133
ClinVar RCV Id: RCV000008609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Gln284Pro
CA250555
NM_001374263.2:c.851A>C