Canonical Allele Identifier: PA2573256054
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1691849
ClinVar RCV Id: RCV002255237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly1322Arg
CA384904441
NM_014191.4:c.3964G>C