Canonical Allele Identifier: PA2826011000
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2010295
ClinVar RCV Id: RCV002850993 RCV003326639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ser1760Pro
CA349068302
NM_001165963.4:c.5278T>C