Canonical Allele Identifier: PA2828361506
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1747203
ClinVar RCV Id: RCV002347163 RCV003096717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Pro1756Ser
CA6571914
NM_001369788.1:c.5266C>T