Canonical Allele Identifier: PA2499278053
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1040115
ClinVar RCV Id: RCV001343699 RCV002508803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Lys1880Glu
CA384888255
NM_014191.4:c.5638A>G