Canonical Allele Identifier: PA658804513
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529866
ClinVar RCV Id: RCV000635368 RCV003451519 RCV003451520 RCV003451521 RCV003456110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Asp646Asn
CA859317
NM_000098.3:c.1936G>A