Canonical Allele Identifier: PA1139724465
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 941314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1827Thr
CA384886661
NM_014191.4:c.5480T>C