Canonical Allele Identifier: PA2827781356
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2796440
ClinVar RCV Id: RCV003753904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ile110Asn
CA349077031
NM_001353957.2:c.329T>A