ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827337621
Gene: PPARG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1337344
ClinVar RCV Id:
RCV001820358
RCV002542613
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317544.2:p.Arg151Gln
CA351618376
NM_001330615.4:c.452G>A