Canonical Allele Identifier: PA2827759321
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93644
ClinVar RCV Id: RCV000079575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Glu1205Lys
CA266837
NM_001353949.2:c.3613G>A