Canonical Allele Identifier: PA2827790786
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 943634
ClinVar RCV Id: RCV001213862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ser1104Tyr
CA349064214
NM_001353961.2:c.3311C>A