Canonical Allele Identifier: PA2828361494
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2851237
ClinVar RCV Id: RCV003754733
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ala1736_Ser1740del
CA2739272037
NM_001369788.1:c.5207_5221del