Allele Registry

Canonical Allele Identifier: PA2826013228

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Gly1343Arg	CA16617292 NM_001165964.3:c.4027G>C