Canonical Allele Identifier: PA2826010225
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2026678
ClinVar RCV Id: RCV002889282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ser1328Ala
CA349052943
NM_001165963.4:c.3982T>G