Canonical Allele Identifier: PA2827291793
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1019242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Val1015Ala
CA384892177
NM_001330260.2:c.3044T>C