Canonical Allele Identifier: PA2827789466
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Val1583Ile
CA285183
NM_001353960.2:c.4747G>A