Canonical Allele Identifier: PA2827761193
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 839613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Glu1687Lys
CA1942695
NM_001353949.2:c.5059G>A