Canonical Allele Identifier: PA916036369
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189901
ClinVar RCV Id: RCV000180853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Trp754Leu
CA303254
NM_001353948.2:c.2261G>T