Allele Registry

Canonical Allele Identifier: PA2826130442

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000239737

ClinVar Variation:

207120

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Ile1438Val	CA318278 NM_001177984.2:c.4312A>G