Canonical Allele Identifier: PA2827291804
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1406775
ClinVar RCV Id: RCV001906987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ala1021Pro
CA6571539
NM_001330260.2:c.3061G>C