Canonical Allele Identifier: PA2828483592
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361191.2:p.Pro10Ala
CA119314
NM_001374262.3:c.28C>G