Canonical Allele Identifier: PA1139723541
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 975895
ClinVar RCV Id: RCV001253024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asp1052Asn
CA384892725
NM_014191.4:c.3154G>A