Canonical Allele Identifier: PA2741866601
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2810635
ClinVar RCV Id: RCV003754115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ala987Thr
CA349060265
NM_001353958.2:c.2959G>A