Canonical Allele Identifier: PA2827772172
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2014067
ClinVar RCV Id: RCV002861311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu1920Ser
CA349063832
NM_001353951.2:c.5759T>C