Canonical Allele Identifier: PA2827292827
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1748805
ClinVar RCV Id: RCV002345134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Val1881Ala
CA384888282
NM_001330260.2:c.5642T>C