Canonical Allele Identifier: PA645421079
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429623
ClinVar RCV Id: RCV000493417 RCV000697208 RCV002527080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Val507Ile
CA859228
NM_000098.3:c.1519G>A