Canonical Allele Identifier: PA1139722563
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 833747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly296Asp
CA385226754
NM_014191.4:c.887G>A