Canonical Allele Identifier: PA2827291604
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 807679
ClinVar RCV Id: RCV000995865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Leu849His
CA384886415
NM_001330260.2:c.2546T>A