Allele Registry

Canonical Allele Identifier: PA2827786262

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059419

ClinVar Variation:

68545

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Tyr1434Cys	CA284964 NM_001353958.2:c.4301A>G