Canonical Allele Identifier: PA2826130201
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 828188
ClinVar RCV Id: RCV001028097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ala1099Thr
CA384893484
NM_001177984.2:c.3295G>A