Canonical Allele Identifier: PA2827784702
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68585
ClinVar RCV Id: RCV000059461 RCV001390614 RCV002381374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Gly343Asp
CA285060
NM_001353958.2:c.1028G>A