Allele Registry

Canonical Allele Identifier: PA119334

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008621

ClinVar Variation:

8144

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Arg194Trp	CA119332 NM_015869.4:c.580C>T