Canonical Allele Identifier: PA2826013323
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 372903
ClinVar RCV Id: RCV000414265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gln1399Leu
CA16042437
NM_001165964.3:c.4196A>T