Canonical Allele Identifier: PA2827756127
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 418590
ClinVar RCV Id: RCV000481626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Leu170Pro
CA16617316
NM_001353949.2:c.509T>C