Canonical Allele Identifier: PA2826011251
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1989927
ClinVar RCV Id: RCV002786755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.His1929Arg
CA349063883
NM_001165963.4:c.5786A>G