Allele Registry

Canonical Allele Identifier: PA303309

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180872

ClinVar Variation:

189920

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Val422Ala	CA303306 NM_006920.6:c.1265T>C