Canonical Allele Identifier: PA891855351
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 568706
ClinVar RCV Id: RCV000689146 RCV001560203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1563Val
CA6571849
NM_014191.4:c.4687A>G