Canonical Allele Identifier: PA2826130162
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 530470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1055Trp
CA6571554
NM_001177984.2:c.3163C>T