Canonical Allele Identifier: PA2827762042
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189893
ClinVar RCV Id: RCV000180845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Arg1916Thr
CA303228
NM_001353949.2:c.5747G>C