Canonical Allele Identifier: PA2830260858
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 2974355
ClinVar RCV Id: RCV003835993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619725.3:p.Val320Ile
CA70184221
NM_138711.6:c.958G>A