Canonical Allele Identifier: PA658669985
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 461346
ClinVar RCV Id: RCV000552965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val1757Ile
CA384885087
NM_014191.4:c.5269G>A