ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827915253
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_001341597.1:p.Ser186Gly
CA351618409
NM_001354668.2:c.556A>G