Canonical Allele Identifier: PA645449225
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 391947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val1031Ala
CA16606571
NM_014191.4:c.3092T>C