Allele Registry

Canonical Allele Identifier: PA2827774191

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Gly1360Arg	CA16617292 NM_001353952.2:c.4078G>C