Canonical Allele Identifier: PA891855393
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 567363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1892His
CA384888449
NM_014191.4:c.5675G>A