Allele Registry

Canonical Allele Identifier: PA1139722540

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001091243

ClinVar Variation:

871344

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Ile268Phe	CA385226553 NM_014191.4:c.802A>T