Canonical Allele Identifier: PA916036393
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 647068
ClinVar RCV Id: RCV000801482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Val840Met
CA349062558
NM_001353948.2:c.2518G>A