Canonical Allele Identifier: PA2827292823
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2575995
ClinVar RCV Id: RCV003322056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ser1879Tyr
CA384888251
NM_001330260.2:c.5636C>A