Canonical Allele Identifier: PA2827784744
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2829623
ClinVar RCV Id: RCV003754413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Gly361Cys
CA349071300
NM_001353958.2:c.1081G>T