Canonical Allele Identifier: PA2826130606
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 253294
ClinVar RCV Id: RCV000239758 RCV000390676 RCV000417005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ala1609Thr
CA10586299
NM_001177984.2:c.4825G>A