Canonical Allele Identifier: PA2827783865
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2813384
ClinVar RCV Id: RCV003754165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ile1754Val
CA349068080
NM_001353957.2:c.5260A>G