Canonical Allele Identifier: PA2828361654
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2703922
ClinVar RCV Id: RCV003589778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Val1909Ile
CA384889896
NM_001369788.1:c.5725G>A