Allele Registry

Canonical Allele Identifier: PA658809610

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636304

ClinVar Variation:

530440

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Asp1755Tyr	CA349068333 NM_001165963.4:c.5263G>T