Canonical Allele Identifier: PA2826013444
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gln1461Lys
CA256608
NM_001165964.3:c.4381C>A