Canonical Allele Identifier: PA317158
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206747
ClinVar RCV Id: RCV000794006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val260Ile
CA317156
NM_001165963.4:c.778G>A