Canonical Allele Identifier: PA119318
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056953.2:p.Pro40Ala
CA119314
NM_015869.4:c.118C>G