Canonical Allele Identifier: PA2827776418
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Arg847His
CA266833
NM_001353954.2:c.2540G>A