Canonical Allele Identifier: PA2827781721
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189962
ClinVar RCV Id: RCV000180916 RCV003588584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Cys336Tyr
CA303417
NM_001353957.2:c.1007G>A