Canonical Allele Identifier: PA915974430
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 794199
ClinVar RCV Id: RCV000977436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Ile725Val
CA6152051
NM_001876.4:c.2173A>G