Canonical Allele Identifier: PA2827789536
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg1619His
CA256584
NM_001353960.2:c.4856G>A