Canonical Allele Identifier: PA2580203461
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1994767
ClinVar RCV Id: RCV002791378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Phe330Leu
CA340394270
NM_001330589.2:c.988T>C
CA340394274
NM_001330589.2:c.990C>A
CA340394275
NM_001330589.2:c.990C>G