Allele Registry

Canonical Allele Identifier: PA3057511936

Gene: PPARG HGNC NCBI

ClinVar RCV:

RCV004736976

RCV005059845

ClinVar Variation:

3353130

HGVS (amino-acid)	Matching Registered Transcripts
NP_619726.3:p.Phe13Leu	CA2258082 NM_138712.5:c.37T>C CA351617434 NM_138712.5:c.39T>G CA351617435 NM_138712.5:c.39T>A