Canonical Allele Identifier: PA1139723086
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 838164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Glu713Asp
CA384879692
NM_014191.4:c.2139A>C
CA384879693
NM_014191.4:c.2139A>T