Canonical Allele Identifier: PA916037007
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68659
ClinVar RCV Id: RCV000059539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ile968Met
CA285234
NM_001353961.2:c.2904C>G