Canonical Allele Identifier: PA2827782542
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68606
ClinVar RCV Id: RCV000059483 RCV001054726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Glu926Lys
CA285102
NM_001353957.2:c.2776G>A