Canonical Allele Identifier: PA2827771939
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374394
ClinVar RCV Id: RCV000414903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Val1773Ala
CA16043651
NM_001353951.2:c.5318T>C