Canonical Allele Identifier: PA285014
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68567
ClinVar RCV Id: RCV000059442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly1751Glu
CA285012
NM_006920.6:c.5252G>A