Canonical Allele Identifier: PA1139725548
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 933726
ClinVar RCV Id: RCV001201997 RCV001255524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.His372Arg
CA340394548
NM_001330589.2:c.1115A>G