Canonical Allele Identifier: PA2826130811
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 567363
ClinVar RCV Id: RCV000687421 RCV000713159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1851His
CA384888449
NM_001177984.2:c.5552G>A