Canonical Allele Identifier: PA2829570482
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_005028.5:p.Phe358Leu
CA119326
NM_005037.7:c.1074T>A
CA351619865
NM_005037.7:c.1072T>C
CA351619868
NM_005037.7:c.1074T>G