Canonical Allele Identifier: PA2828483793
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 436396
ClinVar RCV Id: RCV000503040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Gly131Val
CA351618245
NM_001374263.2:c.392G>T