Canonical Allele Identifier: PA2827780563
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val1600Ile
CA285183
NM_001353955.2:c.4798G>A