Canonical Allele Identifier: PA2827292461
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 573377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Met1600Ile
CA384880261
NM_001330260.2:c.4800G>A
CA384880262
NM_001330260.2:c.4800G>C
CA384880263
NM_001330260.2:c.4800G>T