Canonical Allele Identifier: PA2827790848
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ile1141Met
CA317108
NM_001353961.2:c.3423A>G