Canonical Allele Identifier: PA2828484341
Gene: PPARG HGNC NCBI

Linked Data

ClinVar Variation Id: 8143
ClinVar RCV Id: RCV000008620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361194.1:p.Cys190Ser
CA119330
NM_001374265.1:c.568T>A
CA351618443
NM_001374265.1:c.569G>C