Allele Registry

Canonical Allele Identifier: PA119318

Gene: PPARG HGNC NCBI

ClinVar Allele:

23170

ClinVar RCV:

RCV000008604

RCV000008605

RCV000008606

RCV000008607

ClinVar Variation:

8131

HGVS (amino-acid)	Matching Registered Transcripts
NP_056953.2:p.Pro40Ala	CA119314 NM_015869.4:c.118C>G