Canonical Allele Identifier: PA2827752487
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 194721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala1161Thr
CA240854
NM_001353948.2:c.3481G>A