Allele Registry

Canonical Allele Identifier: PA2825357972

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV002466784

ClinVar Variation:

1803114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001027017.1:p.Arg271Gly	CA381634626 NM_001031847.3:c.811A>G