Canonical Allele Identifier: PA2499251734
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1061998
ClinVar RCV Id: RCV001371666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ser801Pro
CA349071257
NM_001353961.2:c.2401T>C