Canonical Allele Identifier: PA2827292836
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1407277
ClinVar RCV Id: RCV001918359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Thr1888Ser
CA6571937
NM_001330260.2:c.5662A>T
CA384888392
NM_001330260.2:c.5663C>G