Canonical Allele Identifier: PA107997
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68645
ClinVar RCV Id: RCV000059525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1664Lys
CA285198
NM_001165963.4:c.4991T>A