Canonical Allele Identifier: PA2828361371
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 964412
ClinVar RCV Id: RCV001238629 RCV002069309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ile1586Asn
CA384880429
NM_001369788.1:c.4757T>A