Canonical Allele Identifier: PA2827771989
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68662
ClinVar RCV Id: RCV000059542 RCV000193290 RCV000478850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Trp1801Gly
CA206668
NM_001353951.2:c.5401T>G