Canonical Allele Identifier: PA2573255753
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1392047
ClinVar RCV Id: RCV001911150
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly467Ala
CA385228721
NM_014191.4:c.1400G>C