Canonical Allele Identifier: PA2580370344
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1878998
ClinVar RCV Id: RCV002511499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ala446Val
CA385228553
NM_014191.4:c.1337C>T