Canonical Allele Identifier: PA2827292737
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1320728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Met1836Leu
CA236327668
NM_001330260.2:c.5506A>T
CA384886994
NM_001330260.2:c.5506A>C