Canonical Allele Identifier: PA2573256332
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1411036
ClinVar RCV Id: RCV001920417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Lys1934Glu
CA384889514
NM_014191.4:c.5800A>G