Allele Registry

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Canonical Allele Identifier: PA2826009851

Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449377

ClinVar RCV Id: RCV000522963 RCV001315158

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Asp1006Glu	CA1943019 NM_001165963.4:c.3018T>G CA349060373 NM_001165963.4:c.3018T>A