Canonical Allele Identifier: PA205122
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 212135
ClinVar RCV Id: RCV000192357 RCV001857702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile68Val
CA205121
NM_014191.4:c.202A>G