Allele Registry

Canonical Allele Identifier: PA2826260321

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059523

RCV000529623

ClinVar Variation:

68643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Thr1658Met	CA285192 NM_001202435.3:c.4973C>T