Canonical Allele Identifier: PA891855370
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 579919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1827Val
CA6571922
NM_014191.4:c.5479A>G