Canonical Allele Identifier: PA2741942323
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2894009
ClinVar RCV Id: RCV003753026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg278Gln
CA385226620
NM_014191.4:c.833G>A