Canonical Allele Identifier: PA2827754659
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801500
ClinVar RCV Id: RCV003223438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Glu1698Gly
CA349069248
NM_001353948.2:c.5093A>G