Canonical Allele Identifier: PA302744
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 139069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile700Leu
CA302743
NM_014191.4:c.2098A>T
CA384878895
NM_014191.4:c.2098A>C