Canonical Allele Identifier: PA2580370687
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1936334
ClinVar RCV Id: RCV002642539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Pro1945Leu
CA6571959
NM_014191.4:c.5834C>T