Canonical Allele Identifier: PA2827914990
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8143
ClinVar RCV Id: RCV000008620
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341595.2:p.Cys160Ser
CA119330
NM_001354666.3:c.478T>A
CA351618443
NM_001354666.3:c.479G>C