Canonical Allele Identifier: PA2826259783
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 488378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ile1347Asn
CA349050737
NM_001202435.3:c.4040T>A