Canonical Allele Identifier: PA2827290898
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1705682
ClinVar RCV Id: RCV002283996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Thr258Ala
CA385226487
NM_001330260.2:c.772A>G