Canonical Allele Identifier: PA2580370675
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1747203
ClinVar RCV Id: RCV002347163 RCV003096717
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Pro1797Ser
CA6571914
NM_014191.4:c.5389C>T