Canonical Allele Identifier: PA2826013118
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1203729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ala1283Val
CA349053215
NM_001165964.3:c.3848C>T