Canonical Allele Identifier: PA2827782112
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 220200
ClinVar RCV Id: RCV000204396 RCV001753614 RCV002517377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Arg618Cys
CA348628
NM_001353957.2:c.1852C>T