Canonical Allele Identifier: PA2827756465
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408928
ClinVar RCV Id: RCV000476602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ile252Thr
CA16610165
NM_001353949.2:c.755T>C