Canonical Allele Identifier: PA2573090461
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1318574
ClinVar RCV Id: RCV001753349 RCV003772090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Val837Met
CA384884586
NM_014191.4:c.2509G>A