Canonical Allele Identifier: PA106961
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68656
ClinVar RCV Id: RCV000059536 RCV001062878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala175Thr
CA285225
NM_001165963.4:c.523G>A