Canonical Allele Identifier: PA2827784153
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450597
ClinVar RCV Id: RCV000523148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Glu1943Gln
CA349063242
NM_001353957.2:c.5827G>C