Canonical Allele Identifier: PA2826013985
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Glu1767Lys
CA266126
NM_001165964.3:c.5299G>A