Canonical Allele Identifier: PA2741866683
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2861060
ClinVar RCV Id: RCV003752614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ile450Thr
CA349054333
NM_001353961.2:c.1349T>C