Canonical Allele Identifier: PA658807954
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 530447
ClinVar RCV Id: RCV000636317 RCV000658649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Met1836Val
CA6571926
NM_014191.4:c.5506A>G