Allele Registry

Canonical Allele Identifier: PA916036972

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636279

ClinVar Variation:

530420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ala910Val	CA349068800 NM_001353961.2:c.2729C>T