Canonical Allele Identifier: PA2827915112
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1909413
ClinVar RCV Id: RCV002600253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341596.2:p.Lys140Asn
CA351618303
NM_001354667.3:c.420G>C
CA351618304
NM_001354667.3:c.420G>T