Canonical Allele Identifier: PA2741943066
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2575995
ClinVar RCV Id: RCV003322056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ser1879Tyr
CA384888251
NM_014191.4:c.5636C>A