Canonical Allele Identifier: PA2827777934
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Glu1783Lys
CA266126
NM_001353954.2:c.5347G>A