Allele Registry

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Canonical Allele Identifier: PA2827786005

Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 944887

ClinVar RCV Id: RCV001215386

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Arg1297Ser	CA349052983 NM_001353958.2:c.3891A>T CA349052985 NM_001353958.2:c.3891A>C