Canonical Allele Identifier: PA303349
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189933
ClinVar RCV Id: RCV000180886 RCV001255366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1236Pro
CA303346
NM_001165963.4:c.3706G>C