Allele Registry

Canonical Allele Identifier: PA108491

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000013747

RCV000059402

RCV001091670

RCV003992856

ClinVar Variation:

12887

3067167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Trp1204Arg	CA256599 NM_001165963.4:c.3610T>C CA349056162 NM_001165963.4:c.3610T>A