Canonical Allele Identifier: PA2826260837
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1313918
ClinVar RCV Id: RCV001771149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Met1959del
CA2573051700
NM_001202435.3:c.5877_5879del