Canonical Allele Identifier: PA2826260830
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ile1955Met
CA317108
NM_001202435.3:c.5865A>G