Canonical Allele Identifier: PA2827915029
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 1338332
ClinVar RCV Id: RCV001817703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341595.2:p.Asn310Asp
CA351619543
NM_001354666.3:c.928A>G