Canonical Allele Identifier: PA2826258579
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206761
ClinVar RCV Id: RCV000188864 RCV001528187 RCV001857645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Tyr426Cys
CA317209
NM_001202435.3:c.1277A>G