Canonical Allele Identifier: PA2741943054
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2643004
ClinVar RCV Id: RCV003391827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1854Gln
CA236327685
NM_014191.4:c.5561G>A