Canonical Allele Identifier: PA2827771885
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 427057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Gly1746Glu
CA349068318
NM_001353951.2:c.5237G>A