Canonical Allele Identifier: PA2828360952
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 975895
ClinVar RCV Id: RCV001253024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Asp1052Asn
CA384892725
NM_001369788.1:c.3154G>A