Canonical Allele Identifier: PA2827779818
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 194721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ala1149Thr
CA240854
NM_001353955.2:c.3445G>A