Canonical Allele Identifier: PA1139724581
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 976359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.His1931Gln
CA384889475
NM_014191.4:c.5793C>A
CA384889477
NM_014191.4:c.5793C>G