Canonical Allele Identifier: PA2826011093
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 998292
ClinVar RCV Id: RCV001294080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Tyr1809His
CA349067647
NM_001165963.4:c.5425T>C