Canonical Allele Identifier: PA2827756125
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1718615
ClinVar RCV Id: RCV002299940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Leu170His
CA349075607
NM_001353949.2:c.509T>A