Canonical Allele Identifier: PA2741943073
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2892014
ClinVar RCV Id: RCV003752999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Glu1884Lys
CA6571936
NM_014191.4:c.5650G>A