Canonical Allele Identifier: PA916028444
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 638340
ClinVar RCV Id: RCV000790961 RCV003453637 RCV003453634 RCV003453635 RCV003453636
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Arg167Trp
CA858997
NM_001330589.2:c.499C>T