Canonical Allele Identifier: PA2827771090
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_001340880.1:p.Ala1300Val
CA349053215
NM_001353951.2:c.3899C>T