Canonical Allele Identifier: PA2826130741
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 962102
ClinVar RCV Id: RCV001235900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly1798Arg
CA384887082
NM_001177984.2:c.5392G>A
CA384887084
NM_001177984.2:c.5392G>C