Canonical Allele Identifier: PA2827915333
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341599.1:p.Pro12Ala
CA119314
NM_001354670.2:c.34C>G