Allele Registry

Canonical Allele Identifier: PA2827789066

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Gly1342Arg	CA16617292 NM_001353960.2:c.4024G>C