Canonical Allele Identifier: PA2825067407
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2097123
ClinVar RCV Id: RCV003006275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Asp255Val
CA340393626
NM_000098.3:c.764A>T