Canonical Allele Identifier: PA2826130582
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 646657
ClinVar RCV Id: RCV000800992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1588Cys
CA384880442
NM_001177984.2:c.4762C>T