Canonical Allele Identifier: PA2827291859
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 640899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ala1051Val
CA236318583
NM_001330260.2:c.3152C>T