Canonical Allele Identifier: PA2827915209
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8131
ClinVar RCV Id: RCV000008604 RCV000008606 RCV000008605 RCV000008607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341597.1:p.Pro40Ala
CA119314
NM_001354668.2:c.118C>G