Canonical Allele Identifier: PA2828361611
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 423909
ClinVar RCV Id: RCV000482457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Val1859Ala
CA16619567
NM_001369788.1:c.5576T>C