Canonical Allele Identifier: PA2827781505
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 982639
ClinVar RCV Id: RCV001262229 RCV001775164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Gly210Asp
CA349074304
NM_001353957.2:c.629G>A