Canonical Allele Identifier: PA2827789856
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Trp1783Gly
CA206668
NM_001353960.2:c.5347T>G