Allele Registry

Canonical Allele Identifier: PA2825239937

Gene: PPARA HGNC NCBI

ClinVar RCV:

RCV000014700

ClinVar Variation:

13701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001929.1:p.Leu162Val	CA123375 NM_001001929.3:c.484C>G