Canonical Allele Identifier: PA2827333223
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_001317518.1:p.Asp623Asn
CA859317
NM_001330589.2:c.1867G>A