Allele Registry

Canonical Allele Identifier: PA2827786648

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187721

ClinVar RCV:

RCV000180982

ClinVar Variation:

190026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Gly1660Val	CA303590 NM_001353958.2:c.4979G>T