Canonical Allele Identifier: PA2826129533
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 236207
ClinVar RCV Id: RCV000225160 RCV001232816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Leu267Ser
CA10581564
NM_001177984.2:c.800T>C