Allele Registry

Canonical Allele Identifier: PA2826258236

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059457

ClinVar Variation:

68581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ala239Val	CA285051 NM_001202435.3:c.716C>T