Canonical Allele Identifier: PA2827915257
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1337832
ClinVar RCV Id: RCV001822430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341597.1:p.Ser204Pro
CA351618539
NM_001354668.2:c.610T>C