Canonical Allele Identifier: PA2826010202
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 69407
ClinVar RCV Id: RCV001304935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Lys1313Gln
CA59772659
NM_001165963.4:c.3937A>C