Canonical Allele Identifier: PA2828483685
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8143
ClinVar RCV Id: RCV000008620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361191.2:p.Cys160Ser
CA119330
NM_001374262.3:c.478T>A
CA351618443
NM_001374262.3:c.479G>C