Canonical Allele Identifier: PA1139724395
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 846576
ClinVar RCV Id: RCV001049909
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asp1783Val
CA384885463
NM_014191.4:c.5348A>T