Canonical Allele Identifier: PA2827292132
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1472032
ClinVar RCV Id: RCV001975799 RCV003136389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ala1323Ser
CA384904455
NM_001330260.2:c.3967G>T