Canonical Allele Identifier: PA2826130774
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2123352
ClinVar RCV Id: RCV003035370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gln1827Pro
CA384887941
NM_001177984.2:c.5480A>C