Allele Registry

Canonical Allele Identifier: PA123376

Gene: PPARA HGNC NCBI

ClinVar RCV:

RCV000014700

ClinVar Variation:

13701

HGVS (amino-acid)	Matching Registered Transcripts
NP_005027.2:p.Leu162Val	CA123375 NM_005036.5:c.484C>G