Canonical Allele Identifier: PA2827769078
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189956
ClinVar RCV Id: RCV000180910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu108Pro
CA303399
NM_001353951.2:c.323T>C