Canonical Allele Identifier: PA2827915378
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_001341599.1:p.Cys162Ser
CA119330
NM_001354670.2:c.484T>A
CA351618443
NM_001354670.2:c.485G>C