Canonical Allele Identifier: PA658831424
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 546708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1891His
CA384888435
NM_014191.4:c.5672G>A