Canonical Allele Identifier: PA2828483907
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1336956
ClinVar RCV Id: RCV001819442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Arg355Gln
CA2258317
NM_001374263.2:c.1064G>A