Allele Registry

Canonical Allele Identifier: PA2827783822

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000479372

ClinVar Variation:

420677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Pro1731Ser	CA16617281 NM_001353957.2:c.5191C>T