Canonical Allele Identifier: PA2830260928
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619726.3:p.Pro10Ala
CA119314
NM_138712.5:c.28C>G