Canonical Allele Identifier: PA916011814
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 689734
ClinVar RCV Id: RCV000850511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val233Ile
CA385224126
NM_014191.4:c.697G>A