Canonical Allele Identifier: PA2827783922
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Trp1784Gly
CA206668
NM_001353957.2:c.5350T>G