Canonical Allele Identifier: PA2827915254
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8143
ClinVar RCV Id: RCV000008620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341597.1:p.Cys190Ser
CA119330
NM_001354668.2:c.568T>A
CA351618443
NM_001354668.2:c.569G>C