Canonical Allele Identifier: PA916036910
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg834His
CA256584
NM_001353961.2:c.2501G>A