Canonical Allele Identifier: PA2825067489
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2190276
ClinVar RCV Id: RCV002627981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Arg296Gly
CA340394047
NM_000098.3:c.886C>G