Allele Registry

Canonical Allele Identifier: PA3057511859

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV005111817

ClinVar Variation:

3635210

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Ile1631Met	CA384880455 NM_014191.4:c.4893C>G