Canonical Allele Identifier: PA2827777537
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Gly1574Glu
CA285180
NM_001353954.2:c.4721G>A