Canonical Allele Identifier: PA318306
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1932Pro
CA318305
NM_014191.4:c.5795G>C