Canonical Allele Identifier: PA2580203480
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188458
ClinVar RCV Id: RCV002620243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Val380Leu
CA859133
NM_001330589.2:c.1138G>C
CA340394597
NM_001330589.2:c.1138G>T