Canonical Allele Identifier: PA2826130607
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 836368
ClinVar RCV Id: RCV001037482 RCV002275183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ala1609Ser
CA384880647
NM_001177984.2:c.4825G>T