Allele Registry

Canonical Allele Identifier: PA2829854402

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008611

RCV004528094

ClinVar Variation:

8135

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Arg316His	CA250559 NM_015869.4:c.947G>A