Canonical Allele Identifier: PA2828483976
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361193.2:p.Pro10Ala
CA119314
NM_001374264.2:c.28C>G