Allele Registry

Canonical Allele Identifier: PA2826260509

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636304

ClinVar Variation:

530440

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Asp1755Tyr	CA349068333 NM_001202435.3:c.5263G>T