Canonical Allele Identifier: PA2827774974
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1438229
ClinVar RCV Id: RCV001934229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Glu1799Lys
CA349067630
NM_001353952.2:c.5395G>A