Allele Registry

Canonical Allele Identifier: PA2826013394

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059419

ClinVar Variation:

68545

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Tyr1434Cys	CA284964 NM_001165964.3:c.4301A>G