Canonical Allele Identifier: PA2573221978
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1394216
ClinVar RCV Id: RCV001900850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Gly82Arg
CA381637894
NM_001876.4:c.244G>A
CA381637896
NM_001876.4:c.244G>C