Canonical Allele Identifier: PA2827291769
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 932333
ClinVar RCV Id: RCV001200086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Asp989Val
CA384891942
NM_001330260.2:c.2966A>T