Allele Registry

Canonical Allele Identifier: PA2829854411

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008613

ClinVar Variation:

8137

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Val318Met	CA119321 NM_015869.4:c.952G>A