Canonical Allele Identifier: PA2827781382
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2011463
ClinVar RCV Id: RCV002851277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Leu125Val
CA349076791
NM_001353957.2:c.373T>G