Canonical Allele Identifier: PA119334
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8144
ClinVar RCV Id: RCV000008621
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056953.2:p.Arg194Trp
CA119332
NM_015869.4:c.580C>T