Canonical Allele Identifier: PA2827790095
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg1959Gln
CA1942622
NM_001353960.2:c.5876G>A