Canonical Allele Identifier: PA2580203527
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Arg477Gln
CA859200
NM_001330589.2:c.1430G>A