Allele Registry

Canonical Allele Identifier: PA2827781417

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180980

ClinVar Variation:

190024

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Met145Val	CA303585 NM_001353957.2:c.433A>G