ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830260993
Gene: PPARG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2175038
ClinVar RCV Id:
RCV002578919
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_619726.3:p.Ser156Gly
CA351618409
NM_138712.5:c.466A>G