Canonical Allele Identifier: PA2827780501
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1327286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Glu1555Lys
CA59800382
NM_001353955.2:c.4663G>A