Canonical Allele Identifier: PA2499277963
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1042516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Lys718Arg
CA384879727
NM_014191.4:c.2153A>G