Allele Registry

Canonical Allele Identifier: PA3057511857

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV005111815

ClinVar Variation:

3635208

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Ala1603Pro	CA384880278 NM_014191.4:c.4807G>C