Canonical Allele Identifier: PA2827291932
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1031805
ClinVar RCV Id: RCV001333729 RCV002322264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Asp1112Glu
CA384893758
NM_001330260.2:c.3336T>A
CA384893760
NM_001330260.2:c.3336T>G