Allele Registry

Canonical Allele Identifier: PA2827786097

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000798720

RCV003141788

ClinVar Variation:

644737

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Gly1343Cys	CA349050420 NM_001353958.2:c.4027G>T