Canonical Allele Identifier: PA645449049
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 253279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Phe260Ser
CA10586288
NM_014191.4:c.779T>C