Canonical Allele Identifier: PA2573256308
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1380899
ClinVar RCV Id: RCV001895105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1892Leu
CA384888455
NM_014191.4:c.5675G>T