Allele Registry

Canonical Allele Identifier: PA100121

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV000055869

ClinVar Variation:

65656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001867.2:p.Cys304Trp	CA344987 NM_001876.4:c.912C>G