Canonical Allele Identifier: PA2573200830
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352433
ClinVar RCV Id: RCV002047600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Val207Ile
CA22638038
NM_001330589.2:c.619G>A