Canonical Allele Identifier: PA2580203473
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2163113
ClinVar RCV Id: RCV003091616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Phe352Ser
CA340394415
NM_001330589.2:c.1055T>C