Canonical Allele Identifier: PA2827769982
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 498722
ClinVar RCV Id: RCV000591739 RCV001854025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Gln454Lys
CA349070288
NM_001353951.2:c.1360C>A