Canonical Allele Identifier: PA2573255717
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1675496
ClinVar RCV Id: RCV002211225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asn287His
CA385226680
NM_014191.4:c.859A>C