Canonical Allele Identifier: PA2826259552
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 658067
ClinVar RCV Id: RCV000814810 RCV002453849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Thr1210Met
CA1942910
NM_001202435.3:c.3629C>T