Canonical Allele Identifier: PA2827771294
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68541
ClinVar RCV Id: RCV000059415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu1415Arg
CA284952
NM_001353951.2:c.4244T>G