Canonical Allele Identifier: PA2827777917
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374394
ClinVar RCV Id: RCV000414903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Val1772Ala
CA16043651
NM_001353954.2:c.5315T>C