Canonical Allele Identifier: PA2827915246
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1909413
ClinVar RCV Id: RCV002600253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341597.1:p.Lys170Asn
CA351618303
NM_001354668.2:c.510G>C
CA351618304
NM_001354668.2:c.510G>T