Canonical Allele Identifier: PA916037016
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_001340890.1:p.Glu981Lys
CA266126
NM_001353961.2:c.2941G>A