Canonical Allele Identifier: PA2741943033
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2851237
ClinVar RCV Id: RCV003754733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ala1777_Ser1781del
CA2739272037
NM_014191.4:c.5330_5344del