Canonical Allele Identifier: PA1139725521
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 944068
ClinVar RCV Id: RCV001214385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Phe352Leu
CA859116
NM_001330589.2:c.1054T>C
CA340394416
NM_001330589.2:c.1056T>A
CA340394417
NM_001330589.2:c.1056T>G