Canonical Allele Identifier: PA2827291790
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2507235
ClinVar RCV Id: RCV003239126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Lys1012Thr
CA384892157
NM_001330260.2:c.3035A>C