Canonical Allele Identifier: PA2827781890
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1473513
ClinVar RCV Id: RCV002005275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ala420Pro
CA349070867
NM_001353957.2:c.1258G>C