Canonical Allele Identifier: PA916036660
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68618
ClinVar RCV Id: RCV000059495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ser417Thr
CA285132
NM_001353961.2:c.1250G>C