Canonical Allele Identifier: PA2827788561
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_001340889.1:p.Ala986Thr
CA349060265
NM_001353960.2:c.2956G>A