Allele Registry

Canonical Allele Identifier: PA2825357979

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV003068842

ClinVar Variation:

2148517

HGVS (amino-acid)	Matching Registered Transcripts
NP_001027017.1:p.Gly273Ser	CA6152513 NM_001031847.3:c.817G>A