Canonical Allele Identifier: PA100102
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 65640
ClinVar RCV Id: RCV000055853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Arg357Trp
CA344960
NM_001876.4:c.1069C>T