Canonical Allele Identifier: PA2825067485
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2440533
ClinVar RCV Id: RCV003145878 RCV003581893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Ser293Ile
CA340394029
NM_000098.3:c.878G>T