Canonical Allele Identifier: PA1139725588
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 876920
ClinVar RCV Id: RCV001102212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Ser401Ile
CA859143
NM_001330589.2:c.1202G>T