Canonical Allele Identifier: PA2580230137
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2036663
ClinVar RCV Id: RCV002882014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Leu213Pro
CA385224481
NM_001369788.1:c.638T>C