Canonical Allele Identifier: PA2828361582
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2173678
ClinVar RCV Id: RCV002584672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ala1834Val
CA236327758
NM_001369788.1:c.5501C>T