Canonical Allele Identifier: PA2573090470
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1316357
ClinVar RCV Id: RCV001766263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Phe1915Ser
CA384889072
NM_014191.4:c.5744T>C