Canonical Allele Identifier: PA2827782886
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1717863
ClinVar RCV Id: RCV002297858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Met1199Thr
CA349055771
NM_001353957.2:c.3596T>C