Canonical Allele Identifier: PA2826130838
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1029255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Thr1880Ala
CA6571951
NM_001177984.2:c.5638A>G