Allele Registry

Canonical Allele Identifier: PA645404021

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000478580

RCV003338607

ClinVar Variation:

421777

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Met1267Thr	CA16617297 NM_001165963.4:c.3800T>C