Canonical Allele Identifier: PA2580260225
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2156428
ClinVar RCV Id: RCV003090914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Ala306Val
CA6152481
NM_001876.4:c.917C>T