Allele Registry

Canonical Allele Identifier: PA2825239890

Gene: PPARA HGNC NCBI

ClinVar RCV:

RCV000014700

ClinVar Variation:

13701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001928.1:p.Leu162Val	CA123375 NM_001001928.4:c.484C>G