Allele Registry

Canonical Allele Identifier: PA256601

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000013747

RCV000059402

RCV001091670

RCV003992856

ClinVar Variation:

12887

3067167

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Trp1193Arg	CA256599 NM_006920.6:c.3577T>C CA349056162 NM_006920.6:c.3577T>A