Canonical Allele Identifier: PA645449594
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 373225
ClinVar RCV Id: RCV000413396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Glu1963Lys
CA16042906
NM_014191.4:c.5887G>A