Canonical Allele Identifier: PA2827771075
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2153965
ClinVar RCV Id: RCV003069036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu1288Ser
CA1942866
NM_001353951.2:c.3863T>C