Canonical Allele Identifier: PA2826013632
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1524711
ClinVar RCV Id: RCV002049641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ser1587Phe
CA349071250
NM_001165964.3:c.4760C>T