Canonical Allele Identifier: PA2828483881
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1338332
ClinVar RCV Id: RCV001817703
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Asn310Asp
CA351619543
NM_001374263.2:c.928A>G