Allele Registry

Canonical Allele Identifier: PA2826259836

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Gly1371Arg	CA16617292 NM_001202435.3:c.4111G>C