Canonical Allele Identifier: PA1139725536
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956329
ClinVar RCV Id: RCV001229111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Lys354Thr
CA340394429
NM_001330589.2:c.1061A>C