Canonical Allele Identifier: PA2830260885
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8141
ClinVar RCV Id: RCV000008618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619725.3:p.Phe358Leu
CA119326
NM_138711.6:c.1074T>A
CA351619865
NM_138711.6:c.1072T>C
CA351619868
NM_138711.6:c.1074T>G