Canonical Allele Identifier: PA645449578
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 423909
ClinVar RCV Id: RCV000482457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val1900Ala
CA16619567
NM_014191.4:c.5699T>C