Canonical Allele Identifier: PA2741858804
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2607898
ClinVar RCV Id: RCV003345911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Thr501Ile
CA340396609
NM_001330589.2:c.1502C>T