Canonical Allele Identifier: PA645449213
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 192317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asn984Lys
CA10575719
NM_014191.4:c.2952C>G
CA384891868
NM_014191.4:c.2952C>A