Canonical Allele Identifier: PA2827788460
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68524
ClinVar RCV Id: RCV000059396 RCV000429753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Gly921Glu
CA284913
NM_001353960.2:c.2762G>A