Canonical Allele Identifier: PA2826130568
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1335107
ClinVar RCV Id: RCV001816119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile1583Val
CA384880411
NM_001177984.2:c.4747A>G