Canonical Allele Identifier: PA2827783534
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Val1584Ile
CA285183
NM_001353957.2:c.4750G>A