Allele Registry

Canonical Allele Identifier: PA645449049

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000239739

RCV001054624

ClinVar Variation:

253279

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Phe260Ser	CA10586288 NM_014191.4:c.779T>C