Canonical Allele Identifier: PA2826130754
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2643004
ClinVar RCV Id: RCV003391827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1813Gln
CA236327685
NM_001177984.2:c.5438G>A