Canonical Allele Identifier: PA318322
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly1050Ser
CA318321
NM_014191.4:c.3148G>A