Canonical Allele Identifier: PA916028452
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8967
ClinVar RCV Id: RCV000009529 RCV003581557
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Asp213Gly
CA254615
NM_001330589.2:c.638A>G