Canonical Allele Identifier: PA2827787391
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68658
ClinVar RCV Id: RCV000059538 RCV001246264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Gly177Glu
CA285231
NM_001353960.2:c.530G>A