Canonical Allele Identifier: PA2827771606
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1061998
ClinVar RCV Id: RCV001371666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ser1604Pro
CA349071257
NM_001353951.2:c.4810T>C