Canonical Allele Identifier: PA2829353691
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3076914
ClinVar RCV Id: RCV004374690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Val706Met
CA6152096
NM_001876.4:c.2116G>A