Canonical Allele Identifier: PA2580370682
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2430619
ClinVar RCV Id: RCV003129152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ser1879Phe
CA384888247
NM_014191.4:c.5636C>T