Canonical Allele Identifier: PA2826130816
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 836602
ClinVar RCV Id: RCV001037773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ala1858Val
CA384888656
NM_001177984.2:c.5573C>T