Canonical Allele Identifier: PA2827292903
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ser1937Arg
CA318307
NM_001330260.2:c.5809A>C
CA384889605
NM_001330260.2:c.5811C>A
CA384889608
NM_001330260.2:c.5811C>G