Allele Registry

Canonical Allele Identifier: PA2826260332

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000460126

ClinVar Variation:

408926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Met1664Thr	CA16610239 NM_001202435.3:c.4991T>C