Canonical Allele Identifier: PA2580370683
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1748805
ClinVar RCV Id: RCV002345134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val1881Ala
CA384888282
NM_014191.4:c.5642T>C