Canonical Allele Identifier: PA2828360755
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2920015
ClinVar RCV Id: RCV003753881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Tyr810His
CA6571476
NM_001369788.1:c.2428T>C