Canonical Allele Identifier: PA891855388
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 588808
ClinVar RCV Id: RCV002315304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1886Val
CA384888351
NM_014191.4:c.5656A>G