Canonical Allele Identifier: PA2828493228
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1479536
ClinVar RCV Id: RCV001976822 RCV004538707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361195.1:p.Tyr145Cys
CA2258199
NM_001374266.1:c.434A>G