Canonical Allele Identifier: PA2826130808
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1516533
ClinVar RCV Id: RCV002026670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Leu1849Pro
CA384888421
NM_001177984.2:c.5546T>C