Canonical Allele Identifier: PA2573255996
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1462099
ClinVar RCV Id: RCV001968287
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asp1124Glu
CA6571584
NM_014191.4:c.3372T>G
CA384894065
NM_014191.4:c.3372T>A