Canonical Allele Identifier: PA2827787769
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68504
ClinVar RCV Id: RCV000059376 RCV001036662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg393Ser
CA284865
NM_001353960.2:c.1177C>A