Canonical Allele Identifier: PA2827765410
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2010030
ClinVar RCV Id: RCV002850939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ile1019Met
CA349060047
NM_001353950.2:c.3057A>G