Canonical Allele Identifier: PA2825067583
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310133
ClinVar RCV Id: RCV001757201 RCV003451890 RCV003451892 RCV002544074 RCV003451889 RCV003451891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Arg350Gly
CA340394402
NM_000098.3:c.1048C>G