Canonical Allele Identifier: PA2827755885
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 656722
ClinVar RCV Id: RCV000813210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Thr89Ile
CA349077319
NM_001353949.2:c.266C>T