Canonical Allele Identifier: PA1139724502
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 938530
ClinVar RCV Id: RCV001207769 RCV002285455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1866Trp
CA384887871
NM_014191.4:c.5596C>T