Canonical Allele Identifier: PA2827290901
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 253279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Phe260Ser
CA10586288
NM_001330260.2:c.779T>C