Canonical Allele Identifier: PA1139724476
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 954719
ClinVar RCV Id: RCV001227231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1841Pro
CA384887140
NM_014191.4:c.5522G>C