Canonical Allele Identifier: PA2499249761
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011764
ClinVar RCV Id: RCV001309618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.His177Gln
CA340392516
NM_001330589.2:c.531C>A
CA340392517
NM_001330589.2:c.531C>G