Canonical Allele Identifier: PA2573090467
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1320728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Met1836Leu
CA236327668
NM_014191.4:c.5506A>T
CA384886994
NM_014191.4:c.5506A>C