Canonical Allele Identifier: PA2827290901
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 253279
ClinVar RCV Id: RCV000239739 RCV001054624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Phe260Ser
CA10586288
NM_001330260.2:c.779T>C