Canonical Allele Identifier: PA2828360928
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2629005
ClinVar RCV Id: RCV004529715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Lys1032Asn
CA384892407
NM_001369788.1:c.3096G>C
CA384892409
NM_001369788.1:c.3096G>T