Canonical Allele Identifier: PA2830260995
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_619726.3:p.Cys160Ser
CA119330
NM_138712.5:c.478T>A
CA351618443
NM_138712.5:c.479G>C