Canonical Allele Identifier: PA317750
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206927
ClinVar RCV Id: RCV000189071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Thr105Ile
CA317748
NM_001165963.4:c.314C>T