Canonical Allele Identifier: PA2827779571
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Glu942Lys
CA285102
NM_001353955.2:c.2824G>A