Allele Registry

Canonical Allele Identifier: PA2827915255

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008621

ClinVar Variation:

8144

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341597.1:p.Arg194Trp	CA119332 NM_001354668.2:c.580C>T