Canonical Allele Identifier: PA2828483913
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8141
ClinVar RCV Id: RCV000008618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361192.2:p.Phe358Leu
CA119326
NM_001374263.2:c.1074T>A
CA351619865
NM_001374263.2:c.1072T>C
CA351619868
NM_001374263.2:c.1074T>G