Canonical Allele Identifier: PA645449556
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 253296
ClinVar RCV Id: RCV000239760
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Glu1870Asp
CA10586301
NM_014191.4:c.5610A>T
CA384888017
NM_014191.4:c.5610A>C