Canonical Allele Identifier: PA916036790
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_001340890.1:p.Gly619Glu
CA285162
NM_001353961.2:c.1856G>A