Allele Registry

Canonical Allele Identifier: PA2826260623

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002023102

ClinVar Variation:

1512570

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Lys1814del	CA2573133689 NM_001202435.3:c.5440_5442del