Canonical Allele Identifier: PA2828360951
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 640899
ClinVar RCV Id: RCV000794029 RCV002245671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ala1051Val
CA236318583
NM_001369788.1:c.3152C>T