Canonical Allele Identifier: PA2830261114
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8141
ClinVar RCV Id: RCV000008618
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619726.3:p.Phe358Leu
CA119326
NM_138712.5:c.1074T>A
CA351619865
NM_138712.5:c.1072T>C
CA351619868
NM_138712.5:c.1074T>G