Canonical Allele Identifier: PA2826130702
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 846576
ClinVar RCV Id: RCV001049909
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asp1742Val
CA384885463
NM_001177984.2:c.5225A>T