Canonical Allele Identifier: PA107181
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg393Cys
CA284868
NM_001165963.4:c.1177C>T