Allele Registry

Canonical Allele Identifier: PA2827761457

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636358

RCV001956143

ClinVar Variation:

530478

1457986

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Gly1746Arg	CA349068320 NM_001353949.2:c.5236G>C CA349068321 NM_001353949.2:c.5236G>A