Canonical Allele Identifier: PA2830260848
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1336528
ClinVar RCV Id: RCV001817483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619725.3:p.Val305Ile
CA351619509
NM_138711.6:c.913G>A