Canonical Allele Identifier: PA2827767303
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552
ClinVar RCV Id: RCV000059426 RCV000188974 RCV000636318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Cys1577Arg
CA284979
NM_001353950.2:c.4729T>C