Allele Registry

Canonical Allele Identifier: PA2827753315

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000480007

ClinVar Variation:

421697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Gly1371Arg	CA16617292 NM_001353948.2:c.4111G>C