Canonical Allele Identifier: PA2825067339
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2904999
ClinVar RCV Id: RCV003740855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Asp213Ala
CA340393017
NM_000098.3:c.638A>C