Canonical Allele Identifier: PA916012252
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 640559
ClinVar RCV Id: RCV000793606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Thr1887Ala
CA384888366
NM_014191.4:c.5659A>G