Canonical Allele Identifier: PA2829570375
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8143
ClinVar RCV Id: RCV000008620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005028.5:p.Cys160Ser
CA119330
NM_005037.7:c.478T>A
CA351618443
NM_005037.7:c.479G>C