Canonical Allele Identifier: PA2580370271
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1803066
ClinVar RCV Id: RCV002466363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Phe260Val
CA385226500
NM_014191.4:c.778T>G