Canonical Allele Identifier: PA2828361533
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1320728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Met1795Leu
CA236327668
NM_001369788.1:c.5383A>T
CA384886994
NM_001369788.1:c.5383A>C