Canonical Allele Identifier: PA2826130697
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2419005
ClinVar RCV Id: RCV003112249 RCV003154287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Val1730Ile
CA384885264
NM_001177984.2:c.5188G>A