Canonical Allele Identifier: PA2828361608
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1060282
ClinVar RCV Id: RCV001369687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Glu1855Gly
CA6571940
NM_001369788.1:c.5564A>G