Canonical Allele Identifier: PA2499278054
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1060282
ClinVar RCV Id: RCV001369687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Glu1896Gly
CA6571940
NM_014191.4:c.5687A>G