Canonical Allele Identifier: PA2826010186
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2651498
ClinVar RCV Id: RCV003429348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1303Val
CA1942864
NM_001165963.4:c.3908C>T