Canonical Allele Identifier: PA107751
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68600
ClinVar RCV Id: RCV000059477 RCV001548630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.His939Tyr
CA285087
NM_001165963.4:c.2815C>T