Canonical Allele Identifier: PA916011954
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 665233
ClinVar RCV Id: RCV000823470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Tyr724Cys
CA384879771
NM_014191.4:c.2171A>G