Allele Registry

Canonical Allele Identifier: PA915988848

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV000008620

ClinVar Variation:

8143

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Cys190Ser	CA119330 NM_015869.4:c.568T>A CA351618443 NM_015869.4:c.569G>C