Canonical Allele Identifier: PA107619
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68630
ClinVar RCV Id: RCV000059509 RCV000521069 RCV001067468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Gly1433Glu
CA285162
NM_001165963.4:c.4298G>A