Canonical Allele Identifier: PA2827915075
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341596.2:p.Pro10Ala
CA119314
NM_001354667.3:c.28C>G