Canonical Allele Identifier: PA2827784888
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1311030
ClinVar RCV Id: RCV001758539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ala442Gly
CA349070502
NM_001353958.2:c.1325C>G