Allele Registry

Canonical Allele Identifier: PA645404306

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly1371Arg	CA16617292 NM_001165963.4:c.4111G>C