Canonical Allele Identifier: PA2827771771
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801500
ClinVar RCV Id: RCV003223438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Glu1687Gly
CA349069248
NM_001353951.2:c.5060A>G