Allele Registry

Canonical Allele Identifier: PA2827774854

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002044256

ClinVar Variation:

1348315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Val1735Leu	CA1942684 NM_001353952.2:c.5203G>C