Canonical Allele Identifier: PA2573092215
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1336956
ClinVar RCV Id: RCV001819442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056953.2:p.Arg385Gln
CA2258317
NM_015869.4:c.1154G>A