Canonical Allele Identifier: PA2827759564
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408930
ClinVar RCV Id: RCV000475845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Tyr1263Ter