Canonical Allele Identifier: PA645466325
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 373240
ClinVar RCV Id: RCV000413906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Gly465Glu
CA16042851
NM_001876.4:c.1394G>A