Canonical Allele Identifier: PA2580370684
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2500085
ClinVar RCV Id: RCV003224732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly1914Ser
CA384889034
NM_014191.4:c.5740G>A