Canonical Allele Identifier: PA2828361585
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2810214
ClinVar RCV Id: RCV003754106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Pro1837Arg
CA384888230
NM_001369788.1:c.5510C>G