Canonical Allele Identifier: PA2827770932
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801478
ClinVar RCV Id: RCV002463567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Glu1205Gln
CA349056032
NM_001353951.2:c.3613G>C