Canonical Allele Identifier: PA2827292881
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1029255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Thr1921Ala
CA6571951
NM_001330260.2:c.5761A>G