Canonical Allele Identifier: PA2827768717
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Arg1977Gln
CA1942622
NM_001353950.2:c.5930G>A