Canonical Allele Identifier: PA2826010199
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1203729
ClinVar RCV Id: RCV001569863 RCV001866017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1311Val
CA349053215
NM_001165963.4:c.3932C>T