Allele Registry

Canonical Allele Identifier: PA2829210679

Gene: PPARA HGNC NCBI

ClinVar RCV:

RCV000014700

ClinVar Variation:

13701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001380875.1:p.Leu162Val	CA123375 NM_001393946.1:c.484C>G