Allele Registry

Canonical Allele Identifier: PA100065

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV000009632

ClinVar Variation:

9065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001867.2:p.Ala414Val	CA340854 NM_001876.4:c.1241C>T