Canonical Allele Identifier: PA2827332854
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076941
ClinVar RCV Id: RCV004374717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Gln413Lys
CA340394802
NM_001330589.2:c.1237C>A