Canonical Allele Identifier: PA108736
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556
ClinVar RCV Id: RCV000059430 RCV001339387 RCV001781396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1630Met
CA284988
NM_001165963.4:c.4888G>A