Canonical Allele Identifier: PA916037010
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_001340890.1:p.Val970Ala
CA16043651
NM_001353961.2:c.2909T>C