Canonical Allele Identifier: PA2825067258
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2199156
ClinVar RCV Id: RCV002634162 RCV004070839
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Val157Ile
CA858995
NM_000098.3:c.469G>A