Canonical Allele Identifier: PA2825067266
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 638340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Arg167Trp
CA858997
NM_000098.3:c.499C>T