Allele Registry

Canonical Allele Identifier: PA2827760519

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180875

ClinVar Variation:

189923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Ser1505Trp	CA303318 NM_001353949.2:c.4514C>G