Canonical Allele Identifier: PA916036921
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 420883
ClinVar RCV Id: RCV000482880 RCV003221302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Thr844Pro
CA16617285
NM_001353961.2:c.2530A>C