Canonical Allele Identifier: PA2827753151
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Val1335Met
CA284934
NM_001353948.2:c.4003G>A