Canonical Allele Identifier: PA2828361644
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ser1896Arg
CA318307
NM_001369788.1:c.5686A>C
CA384889605
NM_001369788.1:c.5688C>A
CA384889608
NM_001369788.1:c.5688C>G