Canonical Allele Identifier: PA2827786852
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68660
ClinVar RCV Id: RCV000059540 RCV000489760 RCV000764284 RCV000792317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Glu1767Lys
CA266126
NM_001353958.2:c.5299G>A