Canonical Allele Identifier: PA1139724237
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 995251
ClinVar RCV Id: RCV001289208 RCV002537987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1626Leu
CA384880425
NM_014191.4:c.4877G>T