Canonical Allele Identifier: PA2573090449
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1335107
ClinVar RCV Id: RCV001816119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1624Val
CA384880411
NM_014191.4:c.4870A>G