Allele Registry

Canonical Allele Identifier: PA2828483871

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008613

ClinVar Variation:

8137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361192.2:p.Val288Met	CA119321 NM_001374263.2:c.862G>A