Canonical Allele Identifier: PA1139725418
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 970112
ClinVar RCV Id: RCV001245626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Val256Ala
CA340393636
NM_001330589.2:c.767T>C