Canonical Allele Identifier: PA2827764771
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1474345
ClinVar RCV Id: RCV001971204 RCV003147718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ile828Thr
CA349062561
NM_001353950.2:c.2483T>C