Canonical Allele Identifier: PA2827786836
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_001340887.1:p.Val1756Ala
CA16043651
NM_001353958.2:c.5267T>C