Canonical Allele Identifier: PA916012257
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 645276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1904His
CA6571942
NM_014191.4:c.5711G>A