Canonical Allele Identifier: PA108666
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68535
ClinVar RCV Id: RCV000059408 RCV001202491 RCV003352765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1335Met
CA284934
NM_001165963.4:c.4003G>A