Canonical Allele Identifier: PA2741866775
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2715522
ClinVar RCV Id: RCV003590623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Val816Ala
CA349070509
NM_001353961.2:c.2447T>C