Allele Registry

Canonical Allele Identifier: PA2827786132

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180970

RCV003588457

ClinVar Variation:

190014

2734302

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Val1362Leu	CA303554 NM_001353958.2:c.4084G>C CA349050206 NM_001353958.2:c.4084G>T