Canonical Allele Identifier: PA2573256289
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1679326
ClinVar RCV Id: RCV002226923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val1874Leu
CA384888120
NM_014191.4:c.5620G>C
CA384888123
NM_014191.4:c.5620G>T