Canonical Allele Identifier: PA2573200985
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419268
ClinVar RCV Id: RCV001940622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Gly375Ser
CA340394566
NM_001330589.2:c.1123G>A