Canonical Allele Identifier: PA658804507
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529865
ClinVar RCV Id: RCV000635367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Ala361Thr
CA859124
NM_000098.3:c.1081G>A