Allele Registry

Canonical Allele Identifier: PA2829854401

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008609

ClinVar Variation:

8133

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Gln314Pro	CA250555 NM_015869.4:c.941A>C