Canonical Allele Identifier: PA2580203413
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2199156
ClinVar RCV Id: RCV002634162 RCV004070839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Val157Ile
CA858995
NM_001330589.2:c.469G>A