Allele Registry

Canonical Allele Identifier: PA2827786098

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Gly1343Arg	CA16617292 NM_001353958.2:c.4027G>C