Canonical Allele Identifier: PA2580203446
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721974
ClinVar RCV Id: RCV002302308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Ser293Asn
CA859068
NM_001330589.2:c.878G>A